HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
4-Quinolinecarbonyl chloride → N4-[4-(4-amino-1H-imidazo[4,5-c]quinolin-1-yl)butyl]4-quinolinecarboxamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 4-Quinolinecarbonyl chloride | HCID 9990126 | — |
| Edukt | 1-(4-aminobutyl)-1H-imidazo[4,5-c]quinolin-4-amine | HCID 15453775 | — |
| Produkt | N4-[4-(4-amino-1H-imidazo[4,5-c]quinolin-1-yl)butyl]4-quinolinecarboxamide | HCID 12144530 | — |
Reaktionsschritte
According to the general method of Example 14, 1-(4-aminobutyl)-1H-imidazo[4,5-c]quinolin-4-amine and quinoline-4-carbonyl chloride were combined to provide N4-[4-(4-amino-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-4-quinolinecarboxamide as a white crystalline solid, m.p. 214.5-215.2° C. 1H NMR (300 MHz, DMSO-d6) δ 8.89 (d, J=4.3 Hz, 1H), 8.76 (t, J=5.6 Hz, 1H), 8.24 (s, 1H), 8.10-8.01 (m, 3H), 7.78 (ddd, J=8.4, 6.9, 1.5 Hz, 1H), 7.64 (dd, J=8.4, 1.1 Hz, 1H), 7.56 (ddd, J=8.3, 6.9, 1.4 Hz, 1H), 7.44 (ddd, J=8.3, 7.0, 1.3 Hz, 1H), 7.34 (d, J=4.3 Hz, 1H), 7.24 (ddd, J=8.3, 7.0, 1.3 Hz, 1H), 6.60 (broad s, 2H), 4.68 (t, J=6.9 Hz, 2H), 3.38 (q, J=7.0 Hz, 2H), 2.00 (m, 2H), 1.63 (m, 2H); MS (EI) m/e 410.1860 (410.1855 calcd for C24H22N6O).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06756382B2 |
| Quelldatensatz | uspto-grants-2004_06 |
| ORD ID | ord-b9369c50908f4ccf84d18d8158649823 |
| Quellennotiz | uspto-grants-2004_06 |